Mend Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mend Technologies, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Mend Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Dallas, US.
Historical record: 3 cleared submissions from 1988 to 1993. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Mend Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mend Technologies, Inc.
3 devices